134136-23-5

Upstream product

• 79723-95-8 (8-Methoxycarbonyloctyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 100-39-0 benzyl bromide 
• 151896-02-5 9-((2R,3R,4S,5R,6S)-5-Benzyloxy-3,4-dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-nonanoic acid methyl ester 
• 707-07-3 orthobenzoic acid trimethyl ester 
• 74597-40-3 8-(methoxycarbonyl)octyl-α-L-rhamnopyranoside 

Downstream Products

• 134136-25-7 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 134136-29-1 8-(methoxycarbonyl)octyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-4-O-benzyl-α-L-rhamnopyranoside 
• 134136-27-9 8-(methoxycarbonyl)octyl 4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis and n.m.r. analysis of branched trisaccharide and pentasaccharide haptens of the β-hemolytic Streptococci Group A and the preparation of synthetic antigens

The synthesis of branched trisaccharide and pentasaccharide portions of the cell-wall polysaccharide of the β-hemolytic Streptococci Group A is described.The key disaccharide acceptors, allyl or 8-(methoxycarbonyl)octyl 3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-p